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Average Ratings 0 Ratings

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features
design
support

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Write a Review

Description

The Multum database, which encompasses drugs, herbal remedies, and nutraceuticals, stands as a premier resource in the industry aimed at promoting safe medication practices and preventing harmful drug interactions. Its software solutions and databases deliver essential drug information, empowering clinicians to recommend appropriate medications with precise dosages while addressing potential interactions effectively. Lexicon Plus serves as a foundational database, offering extensive drug product and disease terminology that seamlessly connects to our clinical systems and external databases. Additionally, the VantageRx Database is designed in a Microsoft Access format, allowing integration into your applications and providing vital clinical information through multiple database tables. Organizations benefit from development interfaces, ensuring that their unique requirements are addressed. By allowing third-party applications to incorporate specialized functionalities into our software through an open and secure platform, we strive to enhance usability and meet diverse client needs. This integration ultimately aims to improve patient safety and healthcare outcomes.

Description

adWATCH - AE is a solution designed to aid pharmaceutical companies in handling and documenting adverse events that arise during clinical trials. It provides a quick and efficient way for reporters at clinics, hospitals, or investigative sites to create and oversee Adverse Event Reports (AERs), ensuring proper reporting to regulatory bodies and government organizations. An adverse effect refers to a harmful or undesirable reaction experienced by a patient due to medications or medical devices. The process of documenting adverse events necessitates thorough tracking of all medical complaint case details, which culminates in the creation of MedWatch reports, CIOMS reports, and other management documentation. With adWATCH - AE, researchers, physician investigators, Contract Research Organizations (CROs), clinical trial experts, and various health professionals can easily generate and submit AERs in compliance with FDA requirements, adhering to both MedWatch and CIOMS formats. This streamlined process not only enhances regulatory compliance but also improves patient safety oversight during clinical trials.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

Microsoft Access Yes 
Oracle Health Yes 

Integrations

Microsoft Access No 
Oracle Health No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Customer Support

Business Hours No 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) No 
In Person Yes 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person No 

Vendor Details

Company Name

Oracle

Country

United States

Website

www.oracle.com/health/clinical-suite/electronic-health-record/#rc30p4

Vendor Details

Company Name

Atlant Systems

Website

atlantsystems.com/atlant/solutions/atwatch-ae/

Product Features

Product Features

CAPA

Audit Management No 
CAPA Planning No 
Change Management No 
Complaint Management No 
Incident Management No 
Nonconformance Tracking No 
Quality Control No 
Risk Management No 
Root Cause Analysis No 
Training Management No 

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